Variant report

Variant	esv1814312
Chromosome Location	chr17:45611212-45683095
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:301)
CpG islands
(count:123)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr17:45682094-45682251	HepG2	liver:	n/a	n/a
2	CEBPB	chr17:45616239-45616426	H1-hESC	embryonic stem cell:	n/a	chr17:45616275-45616286
3	CEBPB	chr17:45616203-45616429	Hela-S3	cervix:	n/a	chr17:45616275-45616286
4	CEBPB	chr17:45616218-45616423	HepG2	liver:	n/a	chr17:45616275-45616286
5	CEBPB	chr17:45665734-45665783	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr17:45616205-45616431	K562	blood:	n/a	chr17:45616275-45616286
7	CEBPB	chr17:45665732-45665756	K562	blood:	n/a	n/a
8	CEBPB	chr17:45665566-45665892	A549	lung:	n/a	n/a
9	CEBPB	chr17:45616089-45616461	K562	blood:	n/a	chr17:45616275-45616286
10	CEBPB	chr17:45665734-45665763	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr17:45665580-45665831	IMR90	lung:	n/a	n/a
12	CEBPB	chr17:45616208-45616423	IMR90	lung:	n/a	chr17:45616275-45616286
13	CEBPB	chr17:45665577-45665788	HepG2	liver:	n/a	n/a
14	CEBPB	chr17:45616172-45616360	K562	blood:	n/a	chr17:45616275-45616286
15	CEBPB	chr17:45632282-45632410	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr17:45644646-45644894	Hela-S3	cervix:	n/a	chr17:45644788-45644801
17	CTCF	chr17:45639620-45639770	GM12869	blood:	n/a	n/a
18	CTCF	chr17:45639794-45639931	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr17:45639640-45639790	HFF	foreskin:	n/a	n/a
20	CTCF	chr17:45639600-45639750	HAc	cerebellar:	n/a	n/a
21	CTCF	chr17:45639691-45639984	K562	blood:	n/a	n/a
22	CTCF	chr17:45639620-45639770	HepG2	liver:	n/a	n/a
23	CTCF	chr17:45681346-45681457	Medullo	brain:	n/a	n/a
24	CTCF	chr17:45681326-45681405	GM19240	blood:	n/a	n/a
25	CTCF	chr17:45676180-45676330	A549	lung:	n/a	n/a
26	CTCF	chr17:45681300-45681450	Caco-2	colon:	n/a	n/a
27	CTCF	chr17:45655314-45655358	ProgFib	skin:	n/a	n/a
28	CTCF	chr17:45633424-45633495	GM10248	blood:	n/a	n/a
29	CTCF	chr17:45639791-45639953	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr17:45639580-45639730	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr17:45639786-45639888	HepG2	liver:	n/a	n/a
32	CTCF	chr17:45639768-45639951	GM12878	blood:	n/a	n/a
33	CTCF	chr17:45639466-45640016	A549	lung:	n/a	n/a
34	CTCF	chr17:45669308-45669361	MCF-7	breast:	n/a	n/a
35	CTCF	chr17:45639752-45639953	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr17:45639841-45639902	LNCaP	prostate:	n/a	n/a
37	CTCF	chr17:45681260-45681410	AG09319	gingival:	n/a	n/a
38	CTCF	chr17:45639620-45639770	HEK293	kidney:	n/a	n/a
39	CTCF	chr17:45639939-45639941	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr17:45639608-45639654	GM19240	blood:	n/a	n/a
41	CTCF	chr17:45639787-45639938	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr17:45681280-45681430	GM12872	blood:	n/a	n/a
43	CTCF	chr17:45639350-45639422	MCF-7	breast:	n/a	n/a
44	CTCF	chr17:45639653-45639953	A549	lung:	n/a	n/a
45	CTCF	chr17:45681264-45681379	K562	blood:	n/a	n/a
46	CTCF	chr17:45655360-45655510	K562	blood:	n/a	n/a
47	CTCF	chr17:45639761-45639910	MCF-7	breast:	n/a	n/a
48	CTCF	chr17:45682680-45682830	GM06990	blood:	n/a	n/a
49	CTCF	chr17:45639761-45639816	ProgFib	skin:	n/a	n/a
50	CTCF	chr17:45639800-45639917	Spleen_OC	spleen:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45612338-45612388	CMK	blood:	n/a
2	chr17:45612338-45612388	CMK	blood:	n/a
3	chr17:45681383-45681433	SK-N-SH_RA	brain:	n/a
4	chr17:45681383-45681433	HNPCEpiC	eye:	n/a
5	chr17:45681383-45681433	U87	brain:	n/a
6	chr17:45681383-45681433	AG04450	lung:	fetal
7	chr17:45681383-45681433	HRE	kidney:	n/a
8	chr17:45681383-45681433	AG04449	skin:	fetal
9	chr17:45612338-45612388	HCF	heart:	n/a
10	chr17:45681383-45681433	GM06990	blood:	n/a
11	chr17:45612338-45612388	U87	brain:	n/a
12	chr17:45612338-45612388	HEEpiC	esophagus:	n/a
13	chr17:45612338-45612388	MCF-7	breast:	n/a
14	chr17:45612338-45612388	AoSMC	blood vessel:	n/a
15	chr17:45612338-45612388	GM06990	blood:	n/a
16	chr17:45612338-45612388	HNPCEpiC	eye:	n/a
17	chr17:45681383-45681433	HCF	heart:	n/a
18	chr17:45612338-45612388	T-47D	breast:	n/a
19	chr17:45612338-45612388	AG04449	skin:	fetal
20	chr17:45681383-45681433	HCT-116	colon:	n/a
21	chr17:45681383-45681433	MCF-7	breast:	n/a
22	chr17:45681383-45681433	HCPEpiC	choroid plexus:	n/a
23	chr17:45681383-45681433	SKMC	muscle:	n/a
24	chr17:45681383-45681433	HepG2	liver:	n/a
25	chr17:45612338-45612388	HCPEpiC	choroid plexus:	n/a
26	chr17:45681383-45681433	ovcar-3	ovarian:	n/a
27	chr17:45612338-45612388	RPTEC	kidney:	n/a
28	chr17:45612338-45612388	NHBE	bronchial:	n/a
29	chr17:45681383-45681433	T-47D	breast:	n/a
30	chr17:45681383-45681433	BJ	skin:	n/a
31	chr17:45681383-45681433	AG10803	skin:	n/a
32	chr17:45681383-45681433	GM12891	blood:	n/a
33	chr17:45681383-45681433	SK-N-MC	brain:	n/a
34	chr17:45612338-45612388	BJ	skin:	n/a
35	chr17:45612338-45612388	NH-A	brain:	n/a
36	chr17:45612338-45612388	PrEC	prostate:	n/a
37	chr17:45681383-45681433	HL-60	blood:	n/a
38	chr17:45681383-45681433	BE2_C	brain:	n/a
39	chr17:45681383-45681433	K562	blood:	n/a
40	chr17:45681383-45681433	Hela-S3	cervix:	n/a
41	chr17:45681383-45681433	Jurkat	blood:	n/a
42	chr17:45612338-45612388	AG04450	lung:	fetal
43	chr17:45681383-45681433	SK-N-SH	brain:	n/a
44	chr17:45612338-45612388	Jurkat	blood:	n/a
45	chr17:45612338-45612388	HRCEpiC	kidney:	n/a
46	chr17:45681383-45681433	H1-hESC	embryonic stem cell:	embryo
47	chr17:45612338-45612388	AG10803	skin:	n/a
48	chr17:45612338-45612388	PANC-1	pancreas:	n/a
49	chr17:45612338-45612388	AG09319	gingival:	n/a
50	chr17:45681383-45681433	PFSK-1	brain:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45607951..45610083-chr17:45616920..45619918,2	MCF-7	breast:
2	chr17:45681295..45682836-chr17:45684602..45686967,2	MCF-7	breast:
3	chr17:45608528..45610827-chr17:45614421..45616919,2	MCF-7	breast:

No data

Variant related genes	Relation type
NPEPPS	TF binding region
ENSG00000206734	TF binding region
NPEPPS	CpG island
ENSG00000206734	CpG island
ENSG00000141279	chromatin interactions

Extended variants
information (count: 2597 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:2597 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189361759	chr17:45611257-45611258	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs181975258	chr17:45611359-45611360	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs186695531	chr17:45611405-45611406	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192005174	chr17:45611418-45611419	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572424310	chr17:45611485-45611486	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371757670	chr17:45611496-45611497	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541030003	chr17:45611516-45611517	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561322485	chr17:45611518-45611519	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574823341	chr17:45611520-45611521	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543706482	chr17:45611559-45611560	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181277554	chr17:45611580-45611581	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551460205	chr17:45611606-45611607	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564801328	chr17:45611642-45611643	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs527298135	chr17:45611667-45611668	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566232522	chr17:45611679-45611680	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547104634	chr17:45611695-45611696	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs8079821	chr17:45611704-45611705	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs145796837	chr17:45611708-45611709	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs555226031	chr17:45611718-45611719	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs569866632	chr17:45611786-45611787	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538423950	chr17:45611809-45611810	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559024585	chr17:45611815-45611816	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142859928	chr17:45611820-45611821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535098109	chr17:45611847-45611848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573582059	chr17:45611857-45611858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554714587	chr17:45611867-45611868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs151075713	chr17:45611897-45611898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369234168	chr17:45611947-45611948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537866416	chr17:45612009-45612010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200465069	chr17:45612018-45612019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186328049	chr17:45612026-45612027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577046041	chr17:45612027-45612028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190107702	chr17:45612062-45612063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559883615	chr17:45612083-45612084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527440780	chr17:45612198-45612199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547458803	chr17:45612225-45612226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560875316	chr17:45612293-45612294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536093120	chr17:45612311-45612312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs8065938	chr17:45612322-45612323	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs550118049	chr17:45612376-45612377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182105959	chr17:45612473-45612474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186702098	chr17:45612482-45612483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552117896	chr17:45612553-45612554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150385327	chr17:45612567-45612568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534848869	chr17:45612586-45612587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373202819	chr17:45612602-45612603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554606914	chr17:45612645-45612646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372550819	chr17:45612648-45612649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568118341	chr17:45612675-45612676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111656471	chr17:45612785-45612786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Epithelial cancer	20478067	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1110 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45608000-45611400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr17:45609200-45611400	Active TSS	GM12878-XiMat	blood
3	chr17:45609600-45613400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr17:45609800-45611400	Enhancers	Liver	Liver
5	chr17:45609800-45624800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr17:45610000-45617400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr17:45610000-45623400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr17:45610000-45624000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr17:45610000-45624400	Weak transcription	Placenta	Placenta
10	chr17:45610000-45624800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr17:45610000-45630000	Weak transcription	Gastric	stomach
12	chr17:45610000-45638600	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr17:45610000-45639000	Weak transcription	Fetal Muscle Trunk	muscle
14	chr17:45610000-45670600	Weak transcription	Lung	lung
15	chr17:45610000-45670600	Weak transcription	Pancreas	Pancrea
16	chr17:45610000-45676800	Weak transcription	Ovary	ovary
17	chr17:45610200-45674200	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr17:45610400-45611400	Weak transcription	Fetal Intestine Small	intestine
19	chr17:45610400-45611400	Weak transcription	Fetal Muscle Leg	muscle
20	chr17:45610400-45611600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr17:45610400-45617800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr17:45610400-45617800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr17:45610400-45623400	Weak transcription	Duodenum Mucosa	Duodenum
24	chr17:45610400-45624600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr17:45610400-45633800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr17:45610400-45637600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr17:45610400-45637800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr17:45610400-45639200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr17:45610400-45646800	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr17:45610400-45647000	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr17:45610400-45647600	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr17:45610400-45647600	Weak transcription	Osteobl	bone
33	chr17:45610400-45662600	Weak transcription	Adipose Nuclei	Adipose
34	chr17:45610400-45670600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr17:45610600-45611600	Enhancers	HepG2	liver
36	chr17:45610600-45617400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr17:45610600-45617800	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr17:45610600-45623400	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr17:45610600-45623400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr17:45610600-45623400	Weak transcription	Fetal Intestine Large	intestine
41	chr17:45610600-45624000	Weak transcription	Fetal Stomach	stomach
42	chr17:45610600-45624000	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr17:45610600-45624600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr17:45610600-45626400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr17:45610600-45626400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr17:45610600-45637200	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr17:45610600-45647000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr17:45610600-45647000	Weak transcription	Dnd41	blood
49	chr17:45610600-45662200	Weak transcription	HSMM	muscle
50	chr17:45610600-45669200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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